Variant report

Variant	nsv871502
Chromosome Location	chr1:94579426-94607607
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:94586990-94587278	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:94591083-94592179	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:94581863-94582438	HepG2	liver:	n/a	chr1:94582390-94582406 chr1:94582322-94582338
4	BHLHE40	chr1:94591375-94592066	HepG2	liver:	n/a	n/a
5	BRCA1	chr1:94591448-94591557	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:94591151-94591510	ECC-1	luminal epithelium:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
7	CEBPB	chr1:94581945-94582380	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:94591138-94591496	IMR90	lung:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
9	CEBPB	chr1:94581094-94581482	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:94591070-94591576	ECC-1	luminal epithelium:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
11	CEBPB	chr1:94582021-94582349	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:94585460-94585744	HepG2	liver:	n/a	chr1:94585587-94585598 chr1:94585667-94585680
13	CEBPB	chr1:94591162-94591482	Hela-S3	cervix:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
14	CEBPB	chr1:94581188-94581429	A549	lung:	n/a	n/a
15	CEBPB	chr1:94581974-94582341	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:94591475-94591752	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:94591139-94591429	K562	blood:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
18	CEBPB	chr1:94591024-94591600	A549	lung:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
19	CEBPB	chr1:94585448-94585741	IMR90	lung:	n/a	chr1:94585587-94585598 chr1:94585667-94585680
20	CEBPB	chr1:94581224-94581366	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:94591363-94591854	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:94588266-94588381	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:94591405-94591827	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:94591189-94591473	H1-hESC	embryonic stem cell:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
25	CEBPB	chr1:94581100-94581471	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:94591165-94591692	A549	lung:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
27	CEBPB	chr1:94581959-94582348	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:94591132-94591851	HepG2	liver:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
29	CEBPD	chr1:94581976-94582286	HepG2	liver:	n/a	n/a
30	CEBPD	chr1:94591490-94591827	HepG2	liver:	n/a	n/a
31	CEBPD	chr1:94581983-94582231	HepG2	liver:	n/a	n/a
32	CEBPZ	chr1:94591401-94591676	HepG2	liver:	n/a	n/a
33	CHD2	chr1:94591392-94591760	HepG2	liver:	n/a	n/a
34	CHD2	chr1:94586092-94586250	HepG2	liver:	n/a	n/a
35	CHD2	chr1:94581957-94582347	HepG2	liver:	n/a	n/a
36	CREB1	chr1:94581760-94582545	HepG2	liver:	n/a	n/a
37	CREB1	chr1:94581796-94582445	HepG2	liver:	n/a	n/a
38	CTCF	chr1:94591820-94591970	Caco-2	colon:	n/a	n/a
39	CTCF	chr1:94591820-94591970	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr1:94585080-94585230	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr1:94591860-94592010	HepG2	liver:	n/a	n/a
42	CTCF	chr1:94591900-94592050	HRE	kidney:	n/a	n/a
43	CTCF	chr1:94585220-94585370	HMF	breast:	n/a	n/a
44	CTCF	chr1:94596940-94597090	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr1:94585100-94585250	HEK293	kidney:	n/a	n/a
46	CTCF	chr1:94585160-94585310	GM12866	blood:	n/a	n/a
47	CTCF	chr1:94584880-94585030	GM12873	blood:	n/a	n/a
48	CTCF	chr1:94585180-94585330	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr1:94585120-94585270	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr1:94585120-94585270	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94587905-94587955	LNCaP	prostate:	n/a
2	chr1:94587905-94587955	ovcar-3	ovarian:	n/a
3	chr1:94585452-94585502	IMR90	lung:	fetal
4	chr1:94587905-94587955	SK-N-MC	brain:	n/a
5	chr1:94587872-94587922	H1-hESC	embryonic stem cell:	embryo
6	chr1:94586592-94586642	HUVEC	blood vessel:	n/a
7	chr1:94587589-94587639	HRE	kidney:	n/a
8	chr1:94586670-94586720	SK-N-SH_RA	brain:	n/a
9	chr1:94586592-94586642	Hela-S3	cervix:	n/a
10	chr1:94579396-94579446	PFSK-1	brain:	n/a
11	chr1:94579396-94579446	MCF10A-Er-Src	breast:	n/a
12	chr1:94586592-94586642	Caco-2	colon:	n/a
13	chr1:94586670-94586720	HIPEpiC	eye:	n/a
14	chr1:94587905-94587955	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:94587076-94587126	Caco-2	colon:	n/a
16	chr1:94587872-94587922	HUVEC	blood vessel:	n/a
17	chr1:94579396-94579446	NHBE	bronchial:	n/a
18	chr1:94586670-94586720	A549	lung:	n/a
19	chr1:94586670-94586720	HRCEpiC	kidney:	n/a
20	chr1:94587589-94587639	HCPEpiC	choroid plexus:	n/a
21	chr1:94587076-94587126	HCM	heart:	n/a
22	chr1:94585452-94585502	AG10803	skin:	n/a
23	chr1:94587872-94587922	AG09319	gingival:	n/a
24	chr1:94587076-94587126	AG10803	skin:	n/a
25	chr1:94587031-94587081	Hela-S3	cervix:	n/a
26	chr1:94587589-94587639	Caco-2	colon:	n/a
27	chr1:94586592-94586642	HCPEpiC	choroid plexus:	n/a
28	chr1:94585452-94585502	HAEpiC	amniotic membrane:	n/a
29	chr1:94587031-94587081	SK-N-MC	brain:	n/a
30	chr1:94579396-94579446	AG04450	lung:	fetal
31	chr1:94586592-94586642	U87	brain:	n/a
32	chr1:94587905-94587955	IMR90	lung:	fetal
33	chr1:94587076-94587126	AG09309	skin:	n/a
34	chr1:94587076-94587126	Hela-S3	cervix:	n/a
35	chr1:94587589-94587639	MCF10A-Er-Src	breast:	n/a
36	chr1:94579396-94579446	SK-N-SH	brain:	n/a
37	chr1:94587905-94587955	ProgFib	skin:	n/a
38	chr1:94579396-94579446	ProgFib	skin:	n/a
39	chr1:94586670-94586720	ECC-1	luminal epithelium:	n/a
40	chr1:94587905-94587955	NT2-D1	testis:	n/a
41	chr1:94587031-94587081	MCF-7	breast:	n/a
42	chr1:94586670-94586720	Hepatocyte	liver:	n/a
43	chr1:94586670-94586720	HL-60	blood:	n/a
44	chr1:94586670-94586720	SAEC	small airway:	n/a
45	chr1:94586670-94586720	GM06990	blood:	n/a
46	chr1:94579396-94579446	LNCaP	prostate:	n/a
47	chr1:94586670-94586720	HCT-116	colon:	n/a
48	chr1:94587905-94587955	NH-A	brain:	n/a
49	chr1:94587872-94587922	IMR90	lung:	fetal
50	chr1:94586592-94586642	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:94561960..94563528-chr1:94582281..94584718,2	MCF-7	breast:
2	chr1:94573713..94576246-chr1:94579221..94581547,2	MCF-7	breast:
3	chr1:94526939..94529383-chr1:94580613..94583165,2	MCF-7	breast:
4	chr1:94567017..94567580-chr1:94583611..94584143,2	MCF-7	breast:
5	chr1:94564934..94567258-chr1:94582385..94584556,2	MCF-7	breast:
6	chr1:94596499..94598702-chr1:94606759..94609677,2	K562	blood:
7	chr1:94532482..94534156-chr1:94582374..94584202,2	MCF-7	breast:
8	chr1:94596499..94598702-chr1:94606759..94609677,2	K562	blood:
9	chr1:94571469..94574892-chr1:94577789..94583222,4	K562	blood:
10	chr1:94567418..94570803-chr1:94581520..94584135,4	MCF-7	breast:
11	chr1:94586639..94589043-chr1:94594789..94597259,2	MCF-7	breast:
12	chr1:94532251..94537168-chr1:94582958..94586481,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000233482	TF binding region
ABCA4	TF binding region
ENSG00000233482	CpG island
ABCA4	CpG island
ENSG00000198691	chromatin interactions

Extended variants
information (count: 1266 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3789439	chr1:94579426-94579427	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139699862	chr1:94579448-94579449	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs185601748	chr1:94579482-94579483	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs576195661	chr1:94579490-94579491	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs545266674	chr1:94579491-94579492	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs371308038	chr1:94579534-94579535	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs533950783	chr1:94579565-94579566	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs375511778	chr1:94579597-94579598	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs558600933	chr1:94579598-94579599	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs572372199	chr1:94579628-94579629	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74963419	chr1:94579629-94579630	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530123333	chr1:94579666-94579667	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3789440	chr1:94579672-94579673	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs563884047	chr1:94579767-94579768	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4847197	chr1:94579829-94579830	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs143362625	chr1:94579837-94579838	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs372154507	chr1:94579874-94579875	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs566250805	chr1:94579900-94579901	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs190097110	chr1:94579902-94579903	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs547414908	chr1:94579975-94579976	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs567312796	chr1:94579990-94579991	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs528198887	chr1:94579992-94579993	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs376544473	chr1:94579996-94579997	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs11419879	chr1:94580044-94580045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11583439	chr1:94580055-94580056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12025221	chr1:94580059-94580060	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs11805421	chr1:94580065-94580066	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs373919359	chr1:94580091-94580092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569804448	chr1:94580125-94580126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538470982	chr1:94580143-94580144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558776094	chr1:94580168-94580169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550047521	chr1:94580174-94580175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572254752	chr1:94580204-94580205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373184324	chr1:94580210-94580211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12035820	chr1:94580233-94580234	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs532323956	chr1:94580247-94580248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552549143	chr1:94580285-94580286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181797841	chr1:94580332-94580333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543483171	chr1:94580335-94580336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563644583	chr1:94580411-94580412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532696413	chr1:94580444-94580445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546081307	chr1:94580451-94580452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559941103	chr1:94580549-94580550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117829737	chr1:94580625-94580626	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548935656	chr1:94580680-94580681	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs565977150	chr1:94580700-94580701	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560848477	chr1:94580720-94580721	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529738923	chr1:94580775-94580776	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs549814069	chr1:94580813-94580814	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs137895434	chr1:94580825-94580826	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94564600-94591800	Weak transcription	Right Atrium	heart
2	chr1:94567400-94585400	Weak transcription	Brain Anterior Caudate	brain
3	chr1:94571000-94583000	Weak transcription	Pancreas	Pancrea
4	chr1:94571800-94581400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:94574600-94579800	Enhancers	Placenta	Placenta
6	chr1:94574600-94583000	Weak transcription	Brain Substantia Nigra	brain
7	chr1:94575000-94579600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:94575800-94583000	Weak transcription	Left Ventricle	heart
9	chr1:94576400-94581800	Weak transcription	Adipose Nuclei	Adipose
10	chr1:94576800-94582000	Weak transcription	Fetal Muscle Trunk	muscle
11	chr1:94577000-94581200	Weak transcription	Liver	Liver
12	chr1:94577000-94581200	Weak transcription	Spleen	Spleen
13	chr1:94577200-94582000	Weak transcription	Lung	lung
14	chr1:94577400-94581400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr1:94577600-94581200	Enhancers	HepG2	liver
16	chr1:94577600-94582000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:94578400-94579600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr1:94578400-94579600	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:94578400-94579800	Enhancers	Fetal Brain Male	brain
20	chr1:94578400-94581800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr1:94578600-94579800	Enhancers	Fetal Kidney	kidney
22	chr1:94578600-94580000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
23	chr1:94578800-94579600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr1:94578800-94579600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:94578800-94579800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
26	chr1:94578800-94580000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr1:94579000-94579600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:94579000-94579600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr1:94579000-94579600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:94579000-94579600	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr1:94579000-94579800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr1:94579000-94579800	Enhancers	Fetal Muscle Leg	muscle
33	chr1:94579000-94580000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
34	chr1:94579000-94580000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr1:94579000-94580000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr1:94579200-94579600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
37	chr1:94579200-94579800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:94579200-94582400	Weak transcription	Fetal Heart	heart
39	chr1:94579400-94579600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:94579400-94579600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr1:94579400-94579600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:94579400-94579600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:94579400-94579600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
44	chr1:94579400-94579600	Enhancers	Brain Cingulate Gyrus	brain
45	chr1:94579400-94579600	Enhancers	Fetal Thymus	thymus
46	chr1:94579400-94579600	Enhancers	Ovary	ovary
47	chr1:94579400-94579800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr1:94579600-94579800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:94579600-94579800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
50	chr1:94579600-94580400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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